Hi everyone 8 years ago today I got my results Grade 3, pta, I didn’t know if that was good or not, I was ask what treatment I wanted if any, just check ups, ..BCG (didn’t have a clue what that was) or bladder removal, I went with the middle one, once I had the first BCG I had a lovely CNS who was doing it and told me all I needed to know about BC, if only that happened when my results was given it would have saved a lot of worry.
So 8 years on after having 15 BCGs I’m doing well, flexi scopes still every 6 months and I’m happy with that.
Happy New Year one and all and let’s hope 2021 is a lot better than what we’ve just gone through. Stay safe xxx
Happy New Year Sue and 3 cheers for our CNS support teams. Sending love Hx
Hi Sue. I'm a year behind you. So far so good (touch wood). They are still looking after me. Best wishes.
Thanks Sue for posting as a relatively new BC sufferer (2 years) it’s really encouraging to hear good news stories good luck to you long may your good health continue and Happy 2021 to you and yours.
Haha Wilbert, never been called a poster girl before and now I’m too old..or am I lol . Hoping Mr W is well over covid now it must have been very scary for you both.
I don’t know if I’ve just been lucky but can honestly say I’ve not had a problem apart from at the start I was very scared but once I met Angie my CNS all’s been fine.
Good luck to you all whatever treatment your having xxx
Great Sue I am only 18 months clear but great feeling when you see on flexi your clear.
All the best for the future to everyone on this forum.
Rob
Hey Sue/Poster Girl Good to hear from you, & to know that you're doing so well. I'm entering my 9th year of recurrences with just a G2 pTa TCC. After an allergic reaction to MMC in the early days, I'm going to try a 6 week course of Epirubicin on Monday. Didn't we all do well. More drinks are in order I think, to celebrate our good fortune xxx
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